Proximal muscle weakness
Symptom Information:
Symptom ID: | HPO:0003701 | ||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Muscle weakness(HPO:0001324) Proximal muscle weakness(HPO:0003701) MedDRA: |
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Database Frequency: | 105 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
AMYOTROPHIC LATERAL SCLEROSIS 8 | (OMIM:608627) |
AXIAL OSTEOMALACIA | (OMIM:109130) |
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency | (Orphanet:329314) |
Adult-onset proximal spinal muscular atrophy, autosomal dominant | (Orphanet:209335) |
Autosomal dominant Charcot-Marie-Tooth disease type 2K | (Orphanet:99944) |
Autosomal dominant centronuclear myopathy | (Orphanet:169189) |
Autosomal dominant limb-girdle muscular dystrophy type 1B | (Orphanet:264) |
Autosomal dominant limb-girdle muscular dystrophy type 1C | (Orphanet:265) |
Autosomal dominant optic atrophy, classic type | (Orphanet:98673) |
Autosomal dominant spastic paraplegia type 9 | (Orphanet:100990) |
Autosomal recessive Emery-Dreifuss muscular dystrophy | (Orphanet:98855) |
Autosomal recessive ataxia due to ubiquinone deficiency | (Orphanet:139485) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive limb-girdle muscular dystrophy type 2C | (Orphanet:353) |
Autosomal recessive limb-girdle muscular dystrophy type 2D | (Orphanet:62) |
Autosomal recessive limb-girdle muscular dystrophy type 2E | (Orphanet:119) |
Autosomal recessive limb-girdle muscular dystrophy type 2F | (Orphanet:219) |
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Autosomal recessive limb-girdle muscular dystrophy type 2J | (Orphanet:140922) |
Autosomal recessive limb-girdle muscular dystrophy type 2L | (Orphanet:206549) |
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
Autosomal recessive limb-girdle muscular dystrophy type 2N | (Orphanet:206559) |
Autosomal recessive limb-girdle muscular dystrophy type 2O | (Orphanet:206564) |
Autosomal recessive limb-girdle muscular dystrophy type 2Q | (Orphanet:254361) |
Autosomal recessive limb-girdle muscular dystrophy type 2S | (Orphanet:369840) |
Autosomal recessive limb-girdle muscular dystrophy type 2T | (Orphanet:363623) |
Autosomal recessive lower motor neuron disease with childhood onset | (Orphanet:206580) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Bethlem myopathy | (Orphanet:610) |
Cap myopathy | (Orphanet:171881) |
Cardiomyopathy, dilated, 1X | (OMIM:611615) |
Charcot-Marie-Tooth disease type 4B1 | (Orphanet:99955) |
Congenital fiber-type disproportion myopathy | (Orphanet:2020) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Congenital muscular dystrophy with cerebellar involvement | (Orphanet:370959) |
Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
Congenital myasthenic syndromes | (Orphanet:590) |
Desminopathy | (Orphanet:98909) |
Diaphyseal medullary stenosis - bone malignancy | (Orphanet:85182) |
Distal myopathy, Nonaka type | (Orphanet:602) |
EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT | (OMIM:612998) |
EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT | (OMIM:612999) |
EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT | (OMIM:614302) |
EPIPHYSEAL DYSPLASIA, MULTIPLE, 3 | (OMIM:600969) |
Ehlers-Danlos syndrome due to tenascin-X deficiency | (Orphanet:230839) |
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2 | (OMIM:615911) |
Focal myositis | (Orphanet:48918) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Giant axonal neuropathy | (Orphanet:643) |
Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Gyrate atrophy of choroid and retina | (Orphanet:414) |
Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia | (Orphanet:79091) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
Hereditary motor and sensory neuropathy, Okinawa type | (Orphanet:90117) |
Hereditary myoclonus - progressive distal muscular atrophy | (Orphanet:2590) |
Hereditary proximal myopathy with early respiratory failure | (Orphanet:178464) |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 1 | (OMIM:167320) |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 3 | (OMIM:615424) |
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia | (Orphanet:52430) |
Inclusion body myositis | (Orphanet:611) |
Laing distal myopathy | (Orphanet:59135) |
MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE | (OMIM:609456) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 | (OMIM:613156) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 | (OMIM:608840) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 | (OMIM:606612) |
MYASTHENIA GRAVIS | (OMIM:254200) |
MYASTHENIC SYNDROME, CONGENITAL, 13 | (OMIM:614750) |
MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC | (OMIM:616040) |
MYOPATHY WITH ABNORMAL LIPID METABOLISM | (OMIM:255100) |
MYOPATHY WITH EXTRAPYRAMIDAL SIGNS | (OMIM:615673) |
MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA | (OMIM:255140) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION | (OMIM:255310) |
MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET | (OMIM:300718) |
Mitochondrial DNA depletion syndrome, myopathic form | (Orphanet:254875) |
Muscle filaminopathy | (Orphanet:171445) |
Myopathy and diabetes mellitus | (Orphanet:2596) |
Myosclerosis | (Orphanet:289380) |
Myotilin-related myofibrillar myopathy without spheroid body | (Orphanet:98911) |
NARP syndrome | (Orphanet:644) |
NEMALINE MYOPATHY 1 | (OMIM:609284) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
Nemaline myopathy | (Orphanet:607) |
Neutral lipid storage myopathy | (Orphanet:98908) |
Oculopharyngeal muscular dystrophy | (Orphanet:270) |
Oculopharyngodistal myopathy | (Orphanet:98897) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4 | (OMIM:615830) |
PLEOCONIAL MYOPATHY WITH SALT CRAVING | (OMIM:262900) |
POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY | (OMIM:615895) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 | (OMIM:609286) |
PROXIMAL MYOPATHY WITH FOCAL DEPLETION OF MITOCHONDRIA | (OMIM:600706) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Polyglucosan body myopathy type 1 | (ORPHA:397937) |
Proximal myotonic myopathy | (Orphanet:606) |
Proximal spinal muscular atrophy type 4 | (Orphanet:83420) |
Reducing body myopathy | (Orphanet:97239) |
Riboflavin transporter deficiency | (Orphanet:97229) |
SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT | (OMIM:616282) |
Spheroid body myopathy | (Orphanet:268129) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |
Steinert myotonic dystrophy | (Orphanet:273) |
Stormorken-Sjaastad-Langslet syndrome | (Orphanet:3204) |
Tubular aggregate myopathy | (Orphanet:2593) |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH ORWITHOUT MUSCLE WEAKNESS | (OMIM:615441) |
X-linked myopathy with postural muscle atrophy | (Orphanet:178461) |